Necrotic Concentrations of Cisplatin Activate the Apoptotic Machinery but Inhibit Effector Caspases and Interfere with the Execution of Apoptosis

Cisplatin is a chemotherapeutic drug whose cytotoxicity is key to its therapeutic and side effects. Nephrotoxicity, mainly due to renal tubular injury, poses its most important therapeutic limitation. Tubular necrosis is derived from epithelial cell death by apoptosis and necrosis in the proximal an...

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Published in:Toxicological sciences 2011-07, Vol.122 (1), p.73-85
Main Authors: Sancho-Martínez, Sandra M., Piedrafita, F. Javier, Cannata-Andía, Jorge B., López-Novoa, José M., López-Hernández, Francisco J.
Format: Article
Language:English
Subjects:
Antineoplastic Agents - toxicity
Apoptosis - drug effects
bcl-2-Associated X Protein - metabolism
Blotting, Western
Caspase Inhibitors
Cell Death - drug effects
Cisplatin - toxicity
Cytochromes c - metabolism
DNA Fragmentation - drug effects
Enzyme Activation - drug effects
Humans
Male
Mitochondria - drug effects
Mitochondria - metabolism
Necrosis - chemically induced
Necrosis - pathology
Phenotype
Signal Transduction
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Summary:Cisplatin is a chemotherapeutic drug whose cytotoxicity is key to its therapeutic and side effects. Nephrotoxicity, mainly due to renal tubular injury, poses its most important therapeutic limitation. Tubular necrosis is derived from epithelial cell death by apoptosis and necrosis in the proximal and distal tubuli. The mode of cell death has been related to drug concentration, with necrosis occurring with high concentrations and apoptosis with lower concentrations. To fully understand the toxic effects of cisplatin to potentially improve its pharmaco-toxicological profile, it is necessary to unravel the cellular events and signaling pathways implicated in the appearance of both modes of cell death. We used cultured human lymphoma and renal tubule cells to investigate the biochemical and phenotypic characteristics of the death mode induced by increasing concentrations of cisplatin. Our results indicate that pronecrotic concentrations of cisplatin early activate the apoptotic machinery, which is in turn directly blocked by cisplatin at the level of effector caspases. Aborted apoptosis induces a death phenotype lacking some typical characteristics of this process, which more closely resembles necrosis. Furthermore, unidentified Bcl-2- and mitochondria-independent pathways are induced by pronecrotic and not by proapoptotic concentrations of cisplatin. Cisplatin-induced cell necrosis is the result of an aborted apoptosis at the level of effector caspases. Yet, Bcl-2-independent effects lead to cell death, which may pose potential targets for pharmacological intervention aimed at reducing cisplatin nephrotoxicity.
ISSN:1096-6080
1096-0929
DOI:10.1093/toxsci/kfr098